Role Description
The Global Medical Director, Epilepsy Pipeline is a key member of Global Commercialization Organization Medical Affairs (GCOMA) team and reports to the ED, Global Medical Franchise Lead, Epilepsy. This is a strategic role with execution responsibilities, accountable for ensuring the needs and priorities of the US and EUR/INT regions are represented and addressed through engagement with key partners across Jazz.
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Lead the Medical FMT for ABS-1230 and support the epilepsy pipeline including other potential new indications across the epilepsy portfolio.
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Partner closely with US and EUR/INT Medical Affairs teams to understand regional customer, patient, healthcare provider, and healthcare system needs and priorities.
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Represent and advocate for medical perspectives within global cross-functional teams and governance forums, including EDT, LDT, GPT, PGC, and DPRC.
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Contribute Medical Affairs expertise to inform early development activities, including Target Product Profile (TPP) development, clinical trial design and lifecycle planning based on regional insights and aligned future therapeutic landscape scenarios.
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Ensure regional needs and insights are appropriately considered in clinical development discussions, evidence-generation activities, and lifecycle planning.
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Ensure awareness and Medical Affairs functional alignment on clinical development programs.
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Maintain and apply a deep understanding of the competitive landscape to inform evidence generation strategy and internal development decisions.
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Lead the development, maintenance, and execution of the Integrated Evidence Generation Plan (IEGP) for ABS-1230 and other pipeline assets for Jazz.
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Partner effectively across Medical Affairs, Clinical Development, Regulatory Affairs, Market Access, HEOR, RWE, Commercial, and other cross-functional teams to support evidence generation and scientific exchange.
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Lead and support evidence-generation activities, including investigator-sponsored studies, real-world evidence initiatives, health outcomes research, and Phase IV interventional studies, where appropriate.
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Lead the development of the Epilepsy pipeline scientific narrative by identifying and advancing key analytic needs and informing the interpretation of pivotal trial data.
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Lead development of publication strategy in partnership with the Medical Communications team and in alignment with regional evidence needs and scientific priorities.
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Support scientific communications, congress planning, advisory boards, and external engagement activities as required.
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Act as an epilepsy subject matter expert for internal cross-functional stakeholders.
Qualifications
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Significant (10+ years) Medical Affairs, Clinical Development, or related pharmaceutical or biotechnology industry experience, preferably in epilepsy and neuroscience disorders.
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Strong clinical or scientific background in epilepsy therapeutic area.
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Demonstrated experience developing and executing evidence-generation strategies, publication plans, and external scientific engagement activities.
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Strong understanding of clinical research, evidence generation, and neuroscience drug development.
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Proven ability to influence without authority and operate effectively within complex matrix organizations.
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Strong strategic thinking coupled with excellent operational execution skills.
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Excellent written, verbal, presentation, and stakeholder management skills.
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Ability to build productive partnerships across regions and functions and effectively represent diverse stakeholder perspectives.
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Demonstrated ability to manage multiple priorities and deliver high-quality outcomes in a fast-paced environment.
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Experience in lifecycle management of epilepsy/neuroscience indications strongly desired.
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Evidence of success in matrix organizations and track record of high performing behaviors, including independent critical thinking, initiative, and execution under time pressure with competing priorities.
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Self-awareness and emotional intelligence as demonstrated by prior experience navigating complex matrix environments successfully.
Requirements
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Advanced scientific or healthcare degree required (PharmD, PhD, MD, or equivalent).
Benefits
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Discretionary annual cash bonus or incentive compensation (depending on the role).
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Discretionary equity grants in accordance with Jazzβs Long Term Equity Incentive Plan.
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Medical, dental and vision insurance.
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401k retirement savings plan.
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Flexible paid vacation.